The influence of hydrogen bonding on the structure of organic–inorganic hybrid catalysts and its application in the solvent-free epoxidation of α-olefins

In this study, two types of catalysts were prepared by the combination of gemini quaternary ammonium salt with two distinct species of phosphotungstic acid. Catalysts prepared by the Wells–Dawson type of phosphotungstic acid and Keggin-type phosphotungstic acid both exhibited dual-phase catalytic behavior, demonstrating both heterogeneous and homogeneous catalytic activities. In comparison to the catalyst prepared by the Keggin-type phosphotungstic acid, due to the higher size of Wells–Dawson type of phosphotungstic acid, hydrogen bonding could not effectively affect the catalyst prepared by H6P2W18O62. Subsequently, the influential factors on the catalytic reaction were investigated. Through the utilization of techniques such as XPS, FT-IR, Raman spectra and other characterization methods, two distinct structure and reaction mechanisms for these catalysts were elucidated under the influence of hydrogen bonding.


Introduction
Epoxides represent crucial raw materials for the synthesis of ne chemicals, nding extensive applications in nanomaterials, surfactants, food additives, and cosmetics. 1,2Industrially, olen epoxidation has consistently remained the primary method for producing epoxides.The 1,2-epoxy alkanes synthesized by a-olens serve as specic intermediates for synthesizing highvalue chemicals, 3,4 presenting a distinct application potential, particularly in the realm of surfactants. 5,6n the context of olen epoxidation, catalysts have played a pivotal role. 7,8Broadly, these catalysts can be categorized as either metal-based or inorganic catalysts. 9,10Among metalbased catalysts, transition metal-based catalysts have garnered extensive attention owing to their efficient atomic utilization of oxidants. 11Typically, these catalysts are prepared into metalorganic frameworks, 6 polymers, 12,13 phase-transfer catalysts (PTCs), 14 and microemulsions 15 to enhance their catalytic efficiency.The majority of these catalysts are heterogeneous in nature, they may pose certain risks due to the rigorous reaction conditions required for achieving high yields. 16Furthermore, the limited solubility of certain types of homogeneous catalysts under catalytic conditions, along with challenges in separation processes, present signicant hurdles for researchers. 17s a kind of widely used phase-transfer catalysts (PTCs), Ishii-Venturello catalysts 18 have gained widespread use in epoxidation, owing to their mild catalytic conditions and recyclable characteristics. 19Prepared by heteropoly acid and ammonium salt, 20 these catalysts offer a blend of advantages associated with both heterogeneous and homogeneous catalysts.However, the addition of solvents in the catalytic process for catalyst protection contradicts the principles of green chemistry. 21,22Catalysts developed for olen epoxidation under solvent-free conditions were generally only used to oxidize cycloolens 23 or require more stringent reaction conditions. 24onsequently, the present research goals lie in enabling catalysts to function without the addition of solvents.
PTCs prepared by polyoxometalates and Gemini quaternary ammonium salts exhibited an enhanced ability to penetrate the oil-water interface to the oil phase under solvent-free conditions.Not only did they demonstrate exceptional catalytic performance, but also facilitated easier recovery from the reaction system. 25,26Among these catalysts, the utilization of Keggin-type polyoxometalates (POMs) was prevalent due to their outstanding oxidation catalytic performance. 27,28In theory, by the formation of hydrogen bonds in POM, on the one hand, suggesting strong host-guest interactions in two substances could be enhanced, 29 on the other hand, such strong interactions tightened interface contact and accelerated interface electron transfer of catalyst, 30 making the catalytic performance more effective.Wells-Dawson-type phosphotungstic acid, characterized by its nanoscale dimensions of approximately 1 nm, can be viewed as an enhanced Keggin-type cluster, offering a greater number of organic ligands. 31,32Additionally, it provides more redox active sites.Despite these advantages, this species has not been as extensively employed in epoxidation reactions. 33,34n this study, two different types of organic-inorganic composite catalyst was prepared, incorporating Wells-Dawsontype phosphotungstic acid and Keggin-type phosphotungstic acid in combination with a gemini quaternary ammonium salt.Compared with our previous study, 35 due to the addition of hydroxyl groups in the quaternary ammonium salt, the new catalyst prepared by Keggin-type phosphotungstic acid showed distinct microstructure and reaction mechanism.Subsequently, a comparative analysis was performed between catalysts prepared by Keggin type and Wells-Dawson type phosphotungstic acid, leading to the deduction of distinct reaction mechanisms underlying these catalysts.

Synthesis of surfactant DDC
The chemical structure of N1,N3-didodecyl,tetradecyl-2hydroxy-N1,N1,N3,N3-tetramethyl-1,3-propane-diaminium chloride (DDC) was depicted in Scheme 1, which was a type of mixture, with the 3 : 1 molar ratio of dodecylamine to tetradecylamine.The synthesis was conducted under oxygen-free conditions.Specically, 2 mol of 1,3-dichloro-2-propanol were added into a reactor containing 0.4 mol of dodecyl, tetradecyl-dimethylamine in 70 mL of propanol, with a total mass of 0.3 wt% sodium carbonate acting as the catalyst.The reaction mixture was then reuxed at 60 °C for a period of 4-6 hours.Aer the reaction, a white precipitate was obtained through vacuum distillation for solvent removal, followed by 3 times recrystallization using a solvent mixture of ethyl acetate and ethanol (20 : 1).

Synthesis of Wells-Dawson type phosphotungstic acid
Wells-Dawson phosphotungstic acid was synthesized by the documented method: 36 50 g NaWO 4 $2H 2 O was dissolved in 60 mL distilled water, then poured 35.0 mL of concentrated phosphoric acid.The mixture was heated for 20 minutes until it turned milky white, then further heated to 120 °C for 8 hours.Aer the reaction, the mixture was cooled down to room temperature, and a specic quantity of concentrated hydrochloric acid was added to acidify the mixture.Diethyl ether was added to extract the phosphotungstic acid.Upon phase separation, the lower diethyl ether phase, consisted with diethyl ether, water and phosphotungstic acid were selected, and diethyl ether was evaporated under 40 °C conditions.The resulting residue was subjected to drying until a constant weight was achieved, yielding the nal light yellow solid H 6 P 2 W 18 O 62 $14H 2 O. 2.5 Catalyst testing 2.5.1.Catalytic reaction.The selective oxidation of 1dodecene was carried out in a four-neck round ask (250 mL) equipped with a mechanical agitator which provided a 250 rpm stirring rate and a reux condenser.

Catalyst preparation
0.1 mol 1-dodecene, 0.1 mol H 2 O 2 (30% (mass) solution in water), and 5wt% catalysts were added into the ask, the mixture was heated by the heating jacket and stirred by a poly-tetrauoroethylene stirring paddle, besides, a mercurial thermometer was immersed into the solution to make accurate temperature measurements.Due to the different reaction conditions of these 2 catalysts, the specic reaction conditions would be provided in results and discussion.
2.5.2.Gas chromatographic and calculation method.The concentration of a-olen and epoxyalkane were analyzed by gas chromatography (GC-8860A, Angilent, the US) with a ameionization detector and a HP-5 column (35 m × 0.32 mm, lm: 0.5 mm).The temperature of the injector and detector was 300 °C, and 300 °C respectively.The initial temperature of column was 100 °C for 0 minutes, then raised column temperature at 10 °C per minute to 200 °C for 0 minutes, and 50 °C per minute to 320 °C for 5 minutes at the last.High-purity nitrogen was used as the carrier gas.
Analysis of reaction products were used by external standard method.The conversion of a-olen and selectivity of epoxyalkane were calculated according to the formula below: Conversion X = (C 0 − C t )/C 0 , C 0 , C t represents the initial concentration of the reactant and the concentration at time t respectively.Yield g = C pt /C p0 , C pt , C p0 represent the concentration at time t and the theoretical concentration of the product respectively.Selectivity S = g/X.The curves of standard samples were given in ESI (Fig. S1 †).
2.5.3.Catalyst characterization.FT-IR analysis: Fourier transform infrared spectroscopy (FT-IR) was used on a VERTEX 70 spectrophotometer (Bruker, GRE) under a dry air condition at room temperature by the KBr pellets method.Scanning electron microscope (SEM) test was performed on TESCAN MIRA LMS.Elemental analysis was performed on Vario EL CUBE.ICP-MS test was performed on Agilent 5110(OES).X-ray photoelectron spectroscopy (XPS) was performed on Thermo Scientic K-Alpha, and the spectra were charge-corrected using a signal located at 284.5 eV.Small-angle X-ray scattering (SAXS) was performed on SAXSess mc2.UV-vis spectra were performed on Hitachi U4150.Powder XRD was performed on D8 ADVANCE A25.Raman spectra analysis were performed on Horiba Lab-RAM HR Evolution.

Results and discussion
3.1 Catalytic testing 3.1.1.Catalytic performance.Due to the solubility of PW 12 -DDC under high temperature conditions without solvents, the catalytic performance of P 2 W 18 -DDC and PW 12 -DDC in the epoxidation of 1-dodecene was evaluated under the following conditions: 343 K, 1 × 10 −4 mol catalyst dosage, mechanical stirring at 250 rpm, and a 2 : 1 ratio of H 2 O 2 to 1-dodecene, dosage of substrate: 0.1 mol.As depicted in Table 1, aer 6 hours reaction, P 2 W 18 -DDC exhibited higher selectivity towards dodecane epoxide but lower conversion of 1-dodecene compared to PW 12 -DDC.In contrast to PW 12 -DDC, almost all of the P 2 W 18 -DDC catalyst could be recovered aer the reaction.
Subsequently, the catalytic performance of different olens under identical conditions was investigated (Table S1 †).P 2 W 18 -DDC exhibited higher selectivity towards epoxides and lower conversion to olens, especially notable in the case of 1-tetradecene, which showed 93% selectivity to tetradecane epoxide and 36% conversion.In comparison with other catalysts, 37,38 P 2 W 18 -DDC demonstrated superior selectivity in the epoxidation of long-chain olens within a relatively short reaction time (only 6 hours), although with the lower olen conversion.Additionally, a notable advantage of this catalyst was its ability to maintain high catalytic activity under solvent-free conditions and be readily reused through a straightforward ltration process by anhydrous ethanol, thus reducing production costs and aligning with the concept of green chemistry.
3.1.2.Optimization of reaction conditions.P 2 W 18 -DDC exhibited negligible catalytic activity at temperatures below 323 K.The addition of Wells-Dawson type phosphotungstic acid or surfactants individually into the system did not result in any catalytic activity.
Initially, the impact of temperature was examined under other invariant reaction conditions (Fig. 1a), with all reaction times kept six hours.As the temperature surpassed 323 K, the conversion of 1-dodecene exhibited a steady increase, while the selectivity of dodecane epoxide initially rose before subsequently declining.At 333 K, P 2 W 18 -DDC demonstrated an optimal selectivity of 92% towards dodecane epoxide.Moreover, the yield of epoxy dodecane continued to rise as the temperature elevated from 323 K to 353 K. Considering both selectivity and product yield, 343 K was selected as the most suitable temperature for the reaction.
Subsequently, the impact of hydrogen peroxide was examined under 343 K with other invariant reaction conditions.The initial ratio of H 2 O 2 to 1-dodecene was varied from 1 : 1 to 4 : 1.As depicted in Fig. 1b, elevated volumes of hydrogen peroxide led to greater conversion of 1-dodecene but lower selectivity of dodecane epoxide.Notably, the selectivity of dodecane epoxide dropped below 90% when the ratio of hydrogen peroxide to 1dodecene was 2 : 1.Consequently, an initial ratio of 2 : 1 for H 2 O 2 and 1-dodecene was deemed the relatively suitable condition.
Next, the inuence of catalyst dosage was investigated using four different dosage levels, while keeping other conditions constant.As illustrated in Fig. 1c, P 2 W 18 -DDC exhibited the lowest conversion of 1-dodecene, along with the highest Paper RSC Advances selectivity towards epoxy dodecane, at 1 × 10 −4 mol catalyst dosage.With an increase in catalyst dosage, the interfacial tension between oil and water decreased due to the presence of long-chain quaternary ammonium salt.This facilitated the formation of smaller droplets and increased the interface area between water phase and oil phase, thereby enhancing the reaction rate.The conversion of 1-dodecene continued to rise, and the selectivity of epoxy dodecane decreased from 90% to 80% as the catalyst dosage increased from 1 × 10 −4 mol to 2 × 10 −4 mol.This trend indicated that an elevated amount of catalyst also resulted in the formation of by-products.Under the determined appropriate conditions, the inuence of reaction time was investigated for 2 to 6 hours.As depicted in Fig. 1d, the selectivity of epoxy dodecane exhibited a rapid increase as the reaction progressed, reaching its maximum at 6 hours, while the conversion of 1-dodecene increased at a slower rate.
Finally, cycle experiments were conducted under the speci-ed conditions: Catalyst dosage at 1 × 10 −4 mol; rotational speed at 250 rpm; temperature at 343 K; and an initial ratio of H 2 O 2 to 1-dodecene at 2 : 1.The catalyst was subsequently ltered for recycling and washed with anhydrous ethanol at least three times aer each reaction cycle.The outcomes were presented in Fig. 1e.As the P 2 W 18 -DDC catalyst was reused, the conversion of 1-dodecene experienced a gradual reduction, while the selectivity of epoxy dodecane dropped steeply aer three cycles of recycling.These ndings suggested that the catalyst possesses a limited recycling capacity.H 6 P 2 W 18 O 62 . 36Compared with P 2 W 18 -DDC, the crystal face of (110) in PW 12 -DDC still performed a strong diffraction, which could be attribute to the polarization of hydrogen bonding between quaternary ammonium salts and phosphotungstic acid.No obvious diffraction peaks of peroxy structure could be observed, which might because that the crystal faces were covered by alkyl chains. 39,40o further determine the microstructure of the catalyst, SAXS analysis was used to characterize P 2 W 18 -DDC and PW 12 -DDC.In the SAXS pattern presented in Fig. 3a, P 2 W 18 -DDC exhibited two scattering peaks arising from ordered structures, characterized by q values of nm −1 and 0.378 nm −1 , respectively.The nearly 1 : 2 ratio of the q values was indicative of lamellar phases.Conversely, in the SAXS pattern of PW 12 -DDC (Fig. 3b), the q-value ratio was approximately 1 : O1.5 : O4, indicating an irregular layered arrangement.The interlayer spacing (dspacing) was determined from the q 1 value of the rst scattering peak using the formula d 1 = 2p/q 1 .For P 2 W 18 -DDC, the calculated d value was 3.3 nm, while for PW 12 -DDC it was 3.06 nm.This observation suggested that P 2 W 18 -DDC possessed a greater layer spacing, which could be attributed to the larger peroxy structure of Wells-Dawson-type phosphotungstic acid.Furthermore, compared with the previously prepared catalys, 35 quaternary ammonium salts with shorter chain lengths in PW 12 -DDC had performed longer interlayer spacing and more irregular lamellar phases, indicated that with the participation of hydrogen bonding, C-OH in DDC could combine a certain quantity of peroxy phosphotungstic acid, facilitated the binding of a certain quantity of peroxy phosphotungstic acid, resulting in the irregular arrangement between phosphotungstic acid molecules to form PW 12 -DDC, while the larger peroxy structure of Wells-Dawson-type phosphotungstic acid could not accommodate more phosphotungstic acid unit, made the hydrogen bonding ineffective.Due to the enhanced capacity of Wells-Dawson-type phosphotungstic acid to bind quaternary ammonium cations, scanning electron microscopy (SEM) was used to provide detailed micromorphological information.The micrographs of P 2 W 18 -DDC and PW 12 -DDC were presented in Fig. S3 and S4, † respectively.The layered structures of both catalysts were observed, P 2 W 18 -DDC demonstrated a more obvious and denser layered arrangement in comparison to PW 12 -DDC.
3.2.2.Elemental analysis.In theory, 1 mol Wells-Dawson type phosphotungstic acid could theoretically combine with 3 mol surfactant, 1 mol Keggin type phosphotungstic acid could theoretically combine with 1.5 mol surfactant (Table S2 †).To determine the relative content of quaternary ammonium salt and phosphotungstic acid of the catalyst, elemental analysis was performed.The elements of C, N, O, and H were conducted using an elemental analyzer, while analysis of P and W was carried out using ICP-MS.The results were presented in Table 2.The molar ratio of W to O in P 2 W 18 -DDC was approximately 2 : 7, and the molar ratio of P to O was nearly 2 : 39.The molar ratio of P to W was 2 : 11.Moreover, the molar ratio of P to N was nearly 4 : 9, indicating that 1 mol Wells-Dawson type phosphotungstic acid molecule was capable of combining with a maximum of 2.25 mol surfactant DDC molecules.This suggested that the charges carried by Dawson type peroxy phosphotungstic acid was lower than the theoretical calculations.Furthermore, in theory, the molar ratio of W to P in PW 12 -DDC was 4 : 1, N to P was nearly 3 : 1, but in fact W to P in PW 12 -DDC was approximately 10 : 1, N to P was nearly 8 : 1, far greater than the ideal structure reported previously. 37Although it is reported that the peroxy phosphotungstic acid anion would be converted to a more stable structure of PW 11 /PW 12 during the immobilization process, more quaternary ammonium salts combined with Keggin type peroxy phosphotungstic acid in PW 12 -DDC might be attributed to the hydrogen bonding between peroxy phosphotungstic acid and surfactant DDC.

XPS analysis.
The XPS spectra were used to reveal the elemental composition on the surface of catalysts.In the XPS spectra shown in Fig. 5a, the full spectra of P 2 W 18 -DDC exhibited obvious peaks at 531, 284, and 36 eV, corresponding to the O 1s, C 1s, and W 4f signals respectively.Similar peaks were observed for PW 12 -DDC as shown in Fig. 5. Following the peaks separation method described by Zhao, et al. 42 Fig.5b revealed the tting of the W element in the catalyst into ve distinct W 4f peaks.Specically, the peak at 34 eV for W 4f 5/2 were attributed to W 4+ , the peak at 34.9 eV for W 4f 7/2 and 37 eV for W 4f 5/2 were attributed to W 5+ , while the peaks at 35.8 eV for W 4f 7/2 and 37.9 eV for W 4f 5/2 were attributed to W 6+ .The surface elemental content of W 5+ in P 2 W 18 -DDC was approximately 79.71%, with the elemental content of W 4+ was 8.18%.In comparison with Wells-Dawson type phosphotungstic acid, a portion of W on the surface of P 2 W 18 -DDC was reduced to W 5+ , suggesting the disruption of the Wells-Dawson type phosphotungstic acid structure on the surface, which could combine with more negative charges, increase the interaction between surfactant and WO X .But the W 4f signal in PW 12 -DDC in Fig. 5e was divided into 4 peaks, the peak at 34 eV for W 4f 5/2 and the peak 36.1 eV for W 4f 7/2 were attributed to W 4+ , the peak at 34.9 eV for W 4f 5/2 and the peak at 37 eV for W 4f 7/2 were attributed to W 5+ , while the W 6+ species were not observed.
In the O 1s spectra in Fig. 5c and f, the peak tting revealed three distinct peaks, the peak at 529.5 eV was attributed to lattice oxygen, while the peak at 530.5 eV corresponded to highly oxidative oxygen species, the peak at 531.5 eV was attributed to surface oxygen species.The surface O in catalyst could be classied as reaction intermediates and other active O species, such as W(O) 2 and less C-OH of quaternary ammonium salt, while W]O could be attributed to highly oxidative O, which was reported to be closely correlated to surface O, could participate in the reaction by combining O to become an active substance, W-O-W could be attributed to lattice O. 43,44 During the catalytic reaction, only surface oxygen, along with highly oxidative oxygen participate in the reaction process.It was worthy noting that although the relative content of quaternary ammonium salts in PW 12 -DDC was relatively higher than P 2 W 18 -DDC, the content of surface O specie was just 9.36%, lower than 24.87% in P 2 W 18 -DDC, but the content of highly oxidative O specie and FWHM were higher than P 2 W 18 -DDC, which could be attributed to the formation of hydrogen bonding between phosphotungstic acid and surfactant DDC during the preparation of PW 12 -DDC.

Mechanism analysis
3.3.1.SEM analysis aer reaction.The utilized P 2 W 18 -DDC was further categorized into two groups: unwashed (Fig. S5 †) and washed with anhydrous ethanol (Fig. S5 †).Both exhibited distinct lamellar phases, underscoring the catalysts' insolubility in both oil and water phases.In Fig. S5, † it was evident that the majority of olens and epoxides were deposited on the catalyst surface, while the Fig. S6 † illustrated that a signicant portion of 1-dodecene was effectively removed by anhydrous ethanol washing while maintaining the layered accumulation.The SEM picture of utilized PW 12 -DDC was shown in Fig. S7, † although the layered structure could still be observed on the catalyst, the layered phase structure performed less distinct, which could be attributed to the further coverage of quaternary ammonium salts and the loss of phosphotungstic acid.To conrm this conclusion, relevant characterizations were analyzed in the following sections.This reduction in ratio likely contributed to the decrease in catalytic reactivity of catalysts, but the content of highly oxidative O nearly unchanged, indicating the transformation between W(O 2 ) and W]O.Notably, aer the reaction, the content of W 6+ in P 2 W 18 -DDC have been increased with the decreased content of W 4+ (Fig. S9d †), with a narrower FWHM of W 5+ peaks in 34.9 eV.This observation suggested that during the reaction, some of the W 5+ and W 4+ species were oxidized back to higher valence states.Conversely, in the W 4f spectra of PW 12 -DDC (Fig. S9b †), the surface tungsten (W) species of PW 12 -DDC predominantly existed in the +5 valence state or lower.Aer the reaction, a decrease in W 5+ contents have been observed, while the content of highly oxidative O and lattice O increased obviously, indicating the formation of WO X groups instead of the original structure of phosphotungstic acid, 44 leading to the weakening of layered structure observed on the SEM image.3.3.4.UV-vis analysis aer reaction.The UV-visible spectra of P 2 W 18 -DDC are presented in Fig. S10.† Notably, a region of higher energy, ranging from 210 to 230 nm, was observed in Fig. S10a, † which could be attributed to charge transfer between the metal and oxygen species, as also indicated at 238 nm in Fig. S10b.† 45 Aer the reaction of P 2 W 18 -DDC (Fig. S10a †), it is noteworthy that the peak at 300 nm experienced a blue shi to 290 nm.Additionally, the absorption edge extended from approximately 480 nm to 430 nm, indicating the oxidation of the metal center to a relatively higher valence state, conversely, the absorption edge of PW 12 -DDC experienced a subtle red shi, indicating the transfer to a lower valence state of the metal center, which was consistent with the results of XPS analysis.
3.3.5.Raman spectra analysis.The Raman spectra of utilized P 2 W 18 -DDC and PW 12 -DDC were also performed.As depicted in Fig. 7, aer reaction, the disappearance of the peaks at 110 cm −1 (structure of Wells-Dawson type phosphotungstic acid) and 620 cm −1 (vibration of C-O) indicated the formation of more peroxy structure in P 2 W 18 -DDC.However, the PW 12 -DDC showed noticeable change aer reaction (Fig. 8).Firstly, compared with Keggin type phosphotungstic acid (Fig. S11 †), the tungsten correlation peaks at 195, 312 and 552 cm −1 in PW 12 -DDC showed a red shi, which could be contributed the hydrogen bonding between W-O-W and C-OH, 46 while P 2 W 18 -DDC showed a blue shi, indicating the larger groups of peroxy structure in P 2 W 18 -DDC, making the inuence of hydrogen bonding ineffective.It could be observed the peaks at 1445 cm −1 and 2900 cm −1 intensied, leading to the removal of phosphotungstic acid structure.The peaks at 880 and 952 cm −1 have performed a red shi to 895 and 970 cm −1 , indicating the transformation from W(O) 2 to W]O, 47 the blue shi from 552 to 530 cm −1 revealed the transform between W-O c -W and W(O) 2 , while the red shi from 195 to 232 cm −1 , 312 to 331 cm −1 could also conrm this conversion.Furthermore, compared with P 2 W 18 -DDC, two new peaks at 100 cm −1 and 998 cm −1 were observed in the PW 12 -DDC, indicated that during the catalytic reaction, the peroxy structure of catalyst underewent a process of forming WO X groups inuenced by hydrogen bonding between DDC and phosphotungstic acid, 43

Conclusions
In this study, two new types of catalyst was prepared to utilize Wells-Dawson-type phosphotungstic acid and Keggin type phosphotungstic acid combined with a biquaternary ammonium cation.Various characterizations were used to elucidate the fundamental structure of the catalysts.Compared with a catalyst synthesized with Keggin-type phosphotungstic acid, the Wells-Dawson-type phosphotungstic acid catalyst exhibited superior selectivity and recyclability, but lower conversion in the epoxidation of 1-dodecene.Subsequently, the impact of various reaction conditions on catalyst performance was investigated, leading to the determination of optimal reaction conditions under solvent-free circumstances, thereby highlighting its potential industrial applicability.Throughout the course of the reaction, signicant structural alterations in the catalyst were observed.Consequently, a comparative analysis was conducted between the pre-and aer-reaction states, enabling the deduction of the catalytic mechanism inuenced by hydrogen bonds for the catalyst synthesized with Keggin type phosphotungstic acid.Notably, this mechanism revealed a distinct reaction pathway in contrast to catalysts synthesized with Wells-Dawson type phosphotungstic acid.
quaternary ammonium salt and phosphotungstate acid system, leading to the formation of hydrogen bonding between C-OH and W-O c -W, moreover, the new band at 938 cm −1 originally branched from 980 cm −1 for W]O was assignable to the reduced W 5+ species due to the intramolecular charge transfer from quaternary ammonium salt to terminal oxygen of PW.41 Conversely, the peaks at 914, 963, and 1090 cm −1 showed the successful synthesis of Wells-Dawson type of phosphotungstic acid, with the similar peaks in catalyst P 2 W 18 -DDC, they exhibited common corresponding to the vibration of W-O b -W, W]O, and P-O, respectively.In conjunction with the elemental analysis results, treatment with H 2 O 2 resulted in the conversion of partial H 6 P 2 W 18 O 62 into a peroxy structure.No signicant shi was observed in P 2 W 18 -DDC, indicating that the combination of Dawson type phosphotungstic acid and quaternary ammonium salts occurred solely through ionic bonding.Furthermore, both catalysts retained the characteristic peak of W-O c -W, conrming the preservation of their Keggin and Wells-Dawson type phosphotungstic acid structures.

3. 3 . 2 .
FT-IR analysis aer reaction.In the FT-IR spectra of the utilized P 2 W 18 -DDC (Fig.6), the structural features remained largely unaltered aer the reaction.The characteristic peaks at 914, 963, and 1090 cm −1 , attributed to the vibrations of W-O b -W, W]O, and P-O, respectively, were still prominently present.Interestingly, in comparison to aer reaction P 2 W 18 -DDC, the majority of the W]O peaks and -O-Opeaks in PW 12 -DDC nearly vanished (at 980 cm −1 and 820 cm −1 ), leaving only very faint residual peaks, the peak of W-O c -W at 725 cm −1 increased noticeably, which was not observed before. 35The reason for these signicant conversion among W]O, W(O 2 ) and W-O c -W might not only be due to the transformation from W]O to W(O 2 ), the peroxidation from W-O c -W to W(O 2 ) induced by hydrogen bonding also involved in the reaction during the catalytic reaction.Furthermore, the peaks at 1080 cm −1 and 1107 cm −1 also conrmed the formation of hydrogen bonding among the terminal oxygen atoms of PW 12 anions and the quaternary ammonium salt, 45 leading to the redox properties of W species tuned by W-O/H.3.3.3.XPS analysis aer reaction.In the XPS spectra of C 1s in P 2 W 18 -DDC and PW 12 -DDC before and aer reaction (Fig. S8 †), the C-N content of these two catalysts remained basically unchanged, proving that the use of anhydrous ethanol could effectively wash off residual olens and epoxides from the catalyst surface.The XPS spectra of O 1s and W 4f of utilized P 2 W 18 -DDC and PW 12 -DDC were demonstrated in Fig. S9.† Aer reaction, the ratio of surface O (C-OH and W(O 2 )) to lattice O (W-O-W) for the catalyst was lower than before the reaction in both catalysts.

Fig. 5
Fig. 5 (a) The full XPS spectra of the P 2 W 18 -DDC, (b) the W 4f XPS spectra of P 2 W 18 -DDC, (c) the O 1s XPS spectra of P 2 W 18 -DDC (d) the full XPS spectra of the PW 12 -DDC, (e) the W 4f XPS spectra of PW 12 -DDC, (f) the O 1s XPS spectra of PW 12 -DDC.
that the catalyst prepared by Keggin type phosphotungstic acid would work through the above two routes in the catalytic reaction.While there was only one route (W(O 2 ) formed from W]O) worked in catalytic reaction of the catalyst prepared by Wells-Dawson type phosphotungstic acid.

Table 1
The results of direct epoxidation of dodecene catalyzed by different catalyst © 2024 The Author(s).Published by the Royal Society of Chemistry RSC Adv., 2024, 14, 12853-12863 | 12855